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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244204Generated: October 30, 2026

Water → 3-(8-Chloroimidazo[1,5-a]pyrazin-3-yl)-1-(hydroxymethyl)cyclobutanol

https://huagongshe.com/reaction/244204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium SulfiteHCID 24437—
ReactantMethyl morpholine oxideHCID 82029—
Reactant8-Chloro-3-(3-methylenecyclobutyl)imidazo[1,5-a]pyrazineHCID 57681050—
Product3-(8-Chloroimidazo[1,5-a]pyrazin-3-yl)-1-(hydroxymethyl)cyclobutanolHCID 57681096—

Reaction Steps

To a THF solution (170 mL) of 8-chloro-3-(3-methylene-cyclobutyl)-imidazo[1,5-a]pyrazine (3.1 g, 14 mmol), water (18 mL), 50% N-methylmorpholine-N-oxide in water (3.2 mL) and potassium osmate, dehydrate (200 mg, 0.70 mmol) were added and the reaction was allowed to stir at rt for 4 h. Sodium sulfite (8.0 g, 70.0 mmol) was added to the reaction mixture and allowed to stir for 30 min at which point the reaction was concentrated in vacuo. The crude product was extracted from the aqueous with EtOAc. The organics were washed with brine and the combined aqueous washes were back extracted with EtOAc (5×50 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated in vacuo to yield the title compounds as a sticky tan/off-white solid; MS (ES+): m/z 254.17 (100) [MH+], 256.19 (50) [MH+++]; HPLC: tR=1.95 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653268B2
Source datasetuspto-grants-2014_02
ORD IDord-af057f5c2979464d810f72870678601a
Source noteuspto-grants-2014_02